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Impact of virtual reality technology treatment based on mirror neuron theory on upper limb rehabilitation in stroke

Impact of virtual reality technology treatment based on mirror neuron theory on upper limb rehabilitation in stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084611
Enrollment
Unknown
Registered
2024-05-21
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Interventions

Graded motor imagery group:On the basis of conventional rehabilitation treatment, graded motor imagination therapy was performed, once per day, 20min/session, 5 times/ week for 4 weeks.
combined sensory observation group:On the basis of conventional rehabilitation treatment, sensory observation therapy combined with graded motor imagery was performed, once per day, 20min/session, 5 t
VR motor imagery group:On the basis of conventional rehabilitation treatment, receiving virtual reality graded motor imagery therapy, once per day, 20min/session, 5 times /week for 4 weeks.
combined VR sensory observation group:On the basis of conventional rehabilitation treatment, receiving virtual reality sensory observation combined graded motor, once per day, 20min/session, 5 times/

Sponsors

General Hospital of Ningxia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? Age 18-80 years old;The patient is willing to accept the study treatment and sign the informed consent; ? Unilateral hemiplegia patients with ischemic or hemorrhagic cerebrovascular disease confirmed by cerebral CT or MRI scan to meet the classification and diagnostic criteria; ? First occurrence of stroke, the onset time was within 6 months; ? Mini-Mental State Examination (MMSE) =20 points; ? Improved Ashworth grade (upper limbs and hands) =2.

Exclusion criteria

Exclusion criteria: ? Patients with cognitive dysfunction (MMSE=20 points) could not cooperate; ? Patients with symptoms of neglect or visual impairment; ? A history of drug or alcohol abuse. ? severe speech, attention, hearing, vision, intelligence, mental disorders; ? bilateral upper limb dysfunction due to orthopedic or neurological reasons; ? Complicated with epilepsy or failure of vital organs (heart, lung, liver, kidney, etc.), malignant tumors, or other unstable conditions; ? Metal foreign body, suffering from claustrophobia or other MR1-related contraindications.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment for Upper Extremity (FMA-UE);resting-state functional magnetic resonance imaging ;

Secondary

MeasureTime frame
Action Research Arm Test (ARAT);Modified Activities of Daily Living Ability (MBI);

Countries

China

Contacts

Public ContactZhu Ning; Wen Sha

General Hospital of Ningxia Medical University

13995310532@163.com+86 139 9531 0532

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 4, 2026